Canonical Allele Identifier: CA1024327007
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs2066220894

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658531dup , CM000684.2:g.21658531dup GRCh38
NC_000022.10:g.22012820dup , CM000684.1:g.22012820dup GRCh37
NC_000022.9:g.20342820dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+142dup
ENST00000498589.1:n.539+69dup
XM_017029165.1:c.674+69dup XP_016884654.1:n.674+69dup
NR_169729.1:n.1343dup
NR_169730.1:n.1246dup
NR_169731.1:n.432-2306dup
NR_169732.1:n.328+69dup
NR_169733.1:n.386+69dup
NR_169734.1:n.410+69dup